Actively Recruiting
Rapid Escalation of Lipid Lowering Therapy to Reduce Recurrent Cardiovascular Event (REDUCE) All Comers Study
Led by Chinese University of Hong Kong · Updated on 2025-12-31
1000
Participants Needed
1
Research Sites
25 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the impact of frequent monitoring and adjustment of lipid-lowering therapy (LLT) to achieve target low-density lipoprotein cholesterol (LDL-C) levels in patients with hyperlipidemia and cardiovascular disease. The study focuses on patients with acute or chronic coronary syndrome due to atherosclerotic coronary artery disease. Despite guidelines recommending aggressive LDL-C lowering primarily with statins, many patients do not reach their LDL-C goals due to factors like non-adherence and limited use of additional therapies. Participants include patients diagnosed with acute or chronic coronary syndrome caused by atherosclerosis. The study observes how frequent LDL-C testing and timely changes in LLT at a specialist clinic affect LDL-C control. There is no interventional treatment assigned; rather, the study collects data on LDL-C levels and therapy adjustments over time to assess current clinical practice strategies. During the study, LDL-C levels will be measured at baseline and at weeks 8, 26, and 52. Researchers will also monitor participants' achievement of LDL-C targets, adherence to lipid-lowering therapy, tolerability, and any major cardiovascular events. Quality of life will be assessed using the 12-Item Short Form Survey at the same time points. The study is observational, with follow-up lasting up to one year to gather comprehensive data on lipid management and cardiovascular outcomes.
CONDITIONS
Brief Title
Rapid Escalation of LipiD Lowering Therapy to Reduce RecUrrent Cardiovascular Event
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Diagnosis of acute coronary syndrome due to atherosclerotic coronary artery disease
- Diagnosis of chronic coronary syndrome due to atherosclerotic coronary artery disease
You will not qualify if you...
- Unable to provide valid consent by the patient or legal guardian
- Acute coronary syndrome due to causes other than atherosclerotic coronary artery disease
- Psychiatric or severe neurological disorder, cirrhosis, or active malignancy with life expectancy less than 6 months
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 52 weeks
Participants are monitored over time with regular assessments of cholesterol levels and cardiovascular health.
Visits at Baseline, Week 8, Week 26, and Week 52
Trial Site Locations
Total: 1 location
1
Prince of Wales Hospital
Shatin, New Terrritories, Hong Kong, 999077
Actively Recruiting
Research Team
G
Guangming Tan
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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